Drug class
Cephalosporins - 4th Generation
Fourth-generation cephalosporins are an advanced subclass of broad-spectrum, parenteral beta-lactam antibiotics, most prominently represented by cefepime. Read more about Cephalosporins - 4th Generation
12 drugs in this class 11 manufacturers
Drugs in Cephalosporins - 4th Generation
CEFEPIME-DEXTROSE (cefepime HCl in dextrose 5 % in water)
CEFEPIME HCL
CEFEPIME HCL
CEFEPIME HCL
CEFEPIME HCL
MAXIPIME (cefepime HCl)
CEFEPIME HCL
CEFEPIME HCL
Fourth-generation cephalosporins are an advanced subclass of broad-spectrum, parenteral beta-lactam antibiotics, most prominently represented by cefepime.
They exert bactericidal activity by binding to penicillin-binding proteins to disrupt bacterial cell wall peptidoglycan synthesis, while their unique zwitterionic structure enhances outer-membrane penetration and stability against hydrolysis by AmpC and other beta-lactamases.
These agents offer expanded coverage against both gram-positive pathogens, such as methicillin-susceptible *Staphylococcus aureus* and *Streptococcus pneumoniae*, and difficult-to-treat gram-negative organisms, including *Pseudomonas aeruginosa* and Enterobacterales.
Consequently, they serve as critical empirical and targeted therapies for severe, nosocomial infections, including hospital-acquired pneumonia, complicated intra-abdominal and urinary tract infections, skin and skin-structure infections, and febrile neutropenia.
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nih.gov
Fourth-generation cephalosporins are an advanced subclass of broad-spectrum, parenteral beta-lactam antibiotics, most prominently represented by cefepime
-
nih.gov
Fourth-generation cephalosporins are an advanced subclass of broad-spectrum, parenteral beta-lactam antibiotics, most prominently represented by cefepime They exert bactericidal activity by binding to penicillin-binding proteins to disrupt bacterial cell wall peptidoglycan synthesis, while their unique zwitterionic structure enhances outer-membrane penetration and stability against hydrolysis by AmpC and other beta-lactamases These agents offer expanded coverage against both gram-positive pathog...
-
nih.gov
They exert bactericidal activity by binding to penicillin-binding proteins to disrupt bacterial cell wall peptidoglycan synthesis, while their unique zwitterionic structure enhances outer-membrane penetration and stability against hydrolysis by AmpC and other beta-lactamases
-
nih.gov
They exert bactericidal activity by binding to penicillin-binding proteins to disrupt bacterial cell wall peptidoglycan synthesis, while their unique zwitterionic structure enhances outer-membrane penetration and stability against hydrolysis by AmpC and other beta-lactamases
-
nih.gov
These agents offer expanded coverage against both gram-positive pathogens, such as methicillin-susceptible *Staphylococcus aureus* and *Streptococcus pneumoniae*, and difficult-to-treat gram-negative organisms, including *Pseudomonas aeruginosa* and Enterobacterales
-
nih.gov
Consequently, they serve as critical empirical and targeted therapies for severe, nosocomial infections, including hospital-acquired pneumonia, complicated intra-abdominal and urinary tract infections, skin and skin-structure infections, and febrile neutropenia
-
nih.gov
Consequently, they serve as critical empirical and targeted therapies for severe, nosocomial infections, including hospital-acquired pneumonia, complicated intra-abdominal and urinary tract infections, skin and skin-structure infections, and febrile neutropenia
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